Variant Gene N. diseases v DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs11075253
rs11075253
1 16 15054789 intron variant C/A snv 0.22 0.800 1.000 1 2012 2012
dbSNP: rs11644601
rs11644601
4 16 15078261 intron variant T/C snv 0.21 0.700 1.000 1 2016 2016